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7197-96-8 Usage

Uses

2,3-Cycloheptenopyridine may be used in chemical synthesis studies.

Check Digit Verification of cas no

The CAS Registry Mumber 7197-96-8 includes 7 digits separated into 3 groups by hyphens. The first part of the number,starting from the left, has 4 digits, 7,1,9 and 7 respectively; the second part has 2 digits, 9 and 6 respectively.
Calculate Digit Verification of CAS Registry Number 7197-96:
(6*7)+(5*1)+(4*9)+(3*7)+(2*9)+(1*6)=128
128 % 10 = 8
So 7197-96-8 is a valid CAS Registry Number.
InChI:InChI=1/C10H13N/c1-2-5-9-6-4-8-11-10(9)7-3-1/h4,6,8H,1-3,5,7H2

7197-96-8 Well-known Company Product Price

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  • (Code)Product description
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  • Aldrich

  • (197513)  2,3-Cycloheptenopyridine  97%

  • 7197-96-8

  • 197513-1G

  • 682.11CNY

  • Detail
  • Aldrich

  • (197513)  2,3-Cycloheptenopyridine  97%

  • 7197-96-8

  • 197513-1G

  • 682.11CNY

  • Detail
  • Aldrich

  • (197513)  2,3-Cycloheptenopyridine  97%

  • 7197-96-8

  • 197513-1G

  • 682.11CNY

  • Detail
  • Aldrich

  • (197513)  2,3-Cycloheptenopyridine  97%

  • 7197-96-8

  • 197513-1G

  • 682.11CNY

  • Detail

7197-96-8SDS

SAFETY DATA SHEETS

According to Globally Harmonized System of Classification and Labelling of Chemicals (GHS) - Sixth revised edition

Version: 1.0

Creation Date: Aug 16, 2017

Revision Date: Aug 16, 2017

1.Identification

1.1 GHS Product identifier

Product name 2,3-CYCLOHEPTENOPYRIDINE

1.2 Other means of identification

Product number -
Other names Einecs 230-568-7

1.3 Recommended use of the chemical and restrictions on use

Identified uses For industry use only.
Uses advised against no data available

1.4 Supplier's details

1.5 Emergency phone number

Emergency phone number -
Service hours Monday to Friday, 9am-5pm (Standard time zone: UTC/GMT +8 hours).

More Details:7197-96-8 SDS

7197-96-8Relevant articles and documents

Direct synthesis of ring-fused quinolines and pyridines catalyzed byNNHY-ligated manganese complexes (Y = NR2or SR)

Han, Mingyang,Lin, Qing,Liu, Qingbin,Liu, Song,Ma, Ning,Solan, Gregory A.,Sun, Wen-Hua,Wang, Zheng,Yan, Xiuli

, p. 8026 - 8036 (2021/12/27)

Four cationic manganese(i) complexes, [(fac-NNHN)Mn(CO)3]Br (Mn-1-Mn-3) and [(fac-NNHS)Mn(CO)3]Br (Mn-4) (whereNNHis a 5,6,7,8-tetrahydro-8-quinolinamine moiety), have been synthesized and evaluated as catalysts for the direct synthesis of quinolines and pyridines by the reaction of a γ-amino alcohol with a ketone or secondary alcohol;NNHS-ligatedMn-4proved the most effective of the four catalysts. The reactions proceeded well in the presence of catalyst loadings in the range 0.5-5.0 mol% and tolerated diverse functional groups such as alkyl, cycloalkyl, alkoxy, chloride and hetero-aryl. A mechanism involving acceptorless dehydrogenation coupling (ADC) has been proposed on the basis of DFT calculations and experimental evidence. Significantly, this manganese-based catalytic protocol provides a promising green and environmentally friendly route to a wide range of synthetically important substituted monocyclic, bicyclic as well as tricyclicN-heterocycles (including 50 quinoline and 26 pyridine examples) with isolated yields of up to 93%.

Pincerlike manganese complex and preparation method thereof, related ligand and preparation method thereof, catalyst composition and application

-

Paragraph 0159-0165, (2021/07/31)

The invention discloses a pincerlike manganese complex, a preparation method thereof, a ligand for preparation, a preparation method of the ligand, a catalyst composition taking the complex as an active component and application of the catalyst composition. According to the pincerlike manganese complex, a cycloalkyl ring is introduced into a ligand framework, and by regulating and controlling the cyclic tension, flexibility and steric hindrance of the cycloalkyl ring, the reactivity and stability of the manganese metal center can be effectively adjusted, and the catalytic activity and substrate applicability of a manganese metal system are remarkably improved. The catalyst composition taking the pincerlike manganese complex as an active component has the advantages of high catalyst activity, wide substrate application range, mild reaction conditions and the like in the process of preparing quinoline or pyridine derivatives by catalyzing dehydrogenation coupling reaction of o-amino aromatic alcohol or gamma-amino alcohol, ketone or secondary alcohol; and the synthesis advantages of low cost and stable performance are embodied, the operation is simple, and the yield is high.

Palladium acetate-catalyzed one-pot synthesis of mono- And disubstitued pyridines

Mikami, Shunya,Toyota, Masahiro

, p. 1315 - 1321 (2019/08/01)

A Pd-catalyzed one-pot synthesis of mono- and disubstituted pyridines was developed. The substituted pyridines were obtained from ketones or an aldehyde and 1,3-diaminopropane using a combination of catalytic Pd(OAc)2 and Cu(OAc)2. High-concentration reaction conditions enabled this catalytic reaction to be acid-free.

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